申请人:——
公开号:US20040009983A1
公开(公告)日:2004-01-15
The invention is directed to compositions containing physiologically active compounds of general formula (I):
1
wherein R
1
is aryl or heteroaryl; R
2
represents hydrogen, acyl, cyano, halo, lower alkenyl or lower alkyl optionally substituted by a substituent selected from cyano, heteroaryl, heterocycloalkyl, —Z
1
R
8
, —C(═O)—NY
3
Y
4
, —CO
2
R
8
, —NY
3
Y
4
, —N(R
6
)—C(═O)—R
7
, —N(R
6
)—C(═O)—NY
3
Y
4
, —N(R
6
)—C(═O)—OR
7
, —N(R
6
)—SO
2
—R
7
, —N(R
6
)—SO
2
—NY
3
Y
4
and one or more halogen a toms ; R
3
represents hydrogen, aryl, cyano, halo, heteroaryl, lower alkyl, —C(═O)—OR
5
or —C(═O)—NY
3
Y; and X
1
represents N, CH, C-halo, C—CN, C—R
7
, C—NY
3
Y
4
, C—OH, C—Z
2
R
7
, C—C(═O)—OR
5
, C—C(═O)—NY
3
Y
4
, C—N(R
8
)—C(═O)—R
7
, C—SO
2
—NY
3
Y
4
, C—N(R
8
)—SO
2
—R
7
, C-alkenyl, C-alkynyl or C—NO
2
; and their prodrugs, and pharmaceutically acceptable salts and solvates of such compounds and their prodrugs, as well as to novel compounds within the scope of formula (I).
Such compounds and compositions have valuable pharmaceutical properties, in particular the ability to inhibit protein kinases.
这项发明涉及含有一般式(I)中生理活性化合物的组合物:其中R1为芳基或杂芳基;R2代表氢、酰基、氰基、卤素、可选择地由氰基、杂芳基、杂环烷基、—Z1R8、—C(═O)—NY3Y4、—CO2R8、—NY3Y4、—N(R6)—C(═O)—R7、—N(R6)—C(═O)—NY3Y4、—N(R6)—C(═O)—OR7、—N(R6)—SO2—R7、—N(R6)—SO2—NY3Y4和一个或多个卤原子取代的较低烯基或较低烷基;R3代表氢、芳基、氰基、卤素、杂芳基、较低烷基、—C(═O)—OR5或—C(═O)—NY3Y;X1代表N、CH、C-卤素、C—CN、C—R7、C—NY3Y4、C—OH、C—Z2R7、C—C(═O)—OR5、C—C(═O)—NY3Y4、C—N(R8)—C(═O)—R7、C—SO2—NY3Y4、C—N(R8)—SO2—R7、C-烯基、C-炔基或C—NO2;以及它们的前药、这些化合物及其前药的药学上可接受的盐和溶剂,以及在一般式(I)范围内的新化合物。这些化合物和组合物具有有价值的药物特性,特别是抑制蛋白激酶的能力。